abnormal autonomic nervous system physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A functional abnormality of the autonomic nervous system. (Human Phenotype Ontology, HP_0012332)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012332
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Genes

24 genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATXN3 ataxin 3
BRAT1 BRCA1-associated ATM activator 1
CAV1 caveolin 1, caveolae protein, 22kDa
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
ECE1 endothelin converting enzyme 1
EDNRB endothelin receptor type B
GLA galactosidase, alpha
GMPPA GDP-mannose pyrophosphorylase A
HEXB hexosaminidase B (beta polypeptide)
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
LIFR leukemia inhibitory factor receptor alpha
LMNB1 lamin B1
NME1 NME/NM23 nucleoside diphosphate kinase 1
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PRNP prion protein
SCN11A sodium channel, voltage gated, type XI alpha subunit
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SOX10 SRY (sex determining region Y)-box 10
TTR transthyretin
WDR45 WD repeat domain 45